Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928638A>C , CM000685.2:g.154928638A>C | GRCh38 |
| NC_000023.10:g.154156913A>C , CM000685.1:g.154156913A>C | GRCh37 |
| NC_000023.9:g.153810107A>C | NCBI36 |
| NG_011403.1:g.99086T>G | |
| NG_011403.2:g.99086T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5152T>G MANE Select | ENSP00000353393.4:p.Phe1718Val | |
| ENST00000360256.8:c.5152T>G | ENSP00000353393.4:p.Phe1718Val | |
| NM_000132.3:c.5152T>G | NP_000123.1:p.Phe1718Val | |
| XM_011531126.1:c.5047T>G | XP_011529428.1:p.Phe1683Val | |
| NM_000132.4:c.5152T>G MANE Select | NP_000123.1:p.Phe1718Val |